G2Cdb::Search

Search results for: CA1

Disease (8)

Disease Description Nervous effect
D00000121 Chronic nonspherocytic haemolytic anaemia N
D00000122 Pyruvate kinase deficiency N
D00000125 Haemolytic anaemia N
D00000185 Cerebellar ataxia (autosomal dominant) Y
D00000186 Cerebellar ataxia (dominant non-episodic) Y
D00000190 Spinocerebellar ataxia type 14 Y
D00000224 Retinitis pigmentosa N
D00000300 Peutz-Jeghers syndrome N

Gene (24)

Gene Symbol Species Description
G00000071 Atp2b1 Mus musculus ATPase, Ca++ transporting, plasma membrane 1
G00000087 Kcnma1 Mus musculus potassium large conductance calcium-activated channel, subfamily M, alpha member 1
G00000088 Kcna2 Mus musculus potassium voltage-gated channel, shaker-related subfamily, member 2
G00000502 Smarca1 Mus musculus SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1
G00000642 Ncam1 Mus musculus neural cell adhesion molecule 1
G00000703 Ica1 Mus musculus islet cell autoantigen 1
G00001320 ATP2B1 Homo sapiens ATPase, Ca++ transporting, plasma membrane 1
G00001336 KCNMA1 Homo sapiens potassium large conductance calcium-activated channel, subfamily M, alpha member 1
G00001343 ITPR1 Homo sapiens inositol 1,4,5-trisphosphate receptor, type 1
G00001751 SMARCA1 Homo sapiens SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1
G00001891 NCAM1 Homo sapiens neural cell adhesion molecule 1
G00001952 ICA1 Homo sapiens islet cell autoantigen 1, 69kDa
G00002428 SYNE1 Homo sapiens spectrin repeat containing, nuclear envelope 1
G00002481 PRKCG Homo sapiens protein kinase C, gamma
G00002594 Abca13 Mus musculus ATP-binding cassette, sub-family A (ABC1), member 13
G00002712 Atp2a1 Mus musculus ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
G00002733 Atxn10 Mus musculus ataxin 10
G00003056 Fnbp1l Mus musculus formin binding protein 1-like
G00003204 Kcna1 Mus musculus potassium voltage-gated channel, shaker-related subfamily, member 1
G00003205 Kcna3 Mus musculus potassium voltage-gated channel, shaker-related subfamily, member 3
G00005584 ABCA13 Homo sapiens ATP-binding cassette, sub-family A (ABC1), member 13
G00005702 ATP2A1 Homo sapiens ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
G00005793 CA1 Homo sapiens carbonic anhydrase I
G00006046 FNBP1L Homo sapiens formin binding protein 1-like
© G2C 2014. The Genes to Cognition Programme received funding from The Wellcome Trust and the EU FP7 Framework Programmes:
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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